Canonical Allele Identifier: PA645460223
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36239

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Cys221Arg
CA213820
NM_033507.3:c.661T>C